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205 results for “wing pattern”
Figures 14-19 from: Simon E (2013) Preliminary study of wing interference patterns (WIPs) in some species of soft scale (Hemiptera, Sternorrhyncha, Coccoidea, Coccidae). ZooKeys 319: 269-281. https://doi.org/10.3897/zookeys.319.4219
Figures 14-19 - Males with "eliptical" patterns of WIPs, subfamily Eriopeltinae: 14, 15 WIP of Luzulaspis frontalis Green 16–17 WIP of Luzulaspis nemorosa Koteja. 18–19 WIP of Eriopeltis lichtensteini Signoret.
Figures 1-5 from: Simon E (2013) Preliminary study of wing interference patterns (WIPs) in some species of soft scale (Hemiptera, Sternorrhyncha, Coccoidea, Coccidae). ZooKeys 319: 269-281. https://doi.org/10.3897/zookeys.319.4219
Figures 1-5 - 1 General scheme of the fore wing (after Koteja 2008) acp-alar cupolae, afx-anterior flexing patch, alf-alar fold, alp-alar lobe, asfd-anterior subcostal field, ast-alar setae, clfd-claval (anal) field, cofd-costal field or thickening, cufd-cubital field, cur-cubital ridge, mat-macrotrichia, mit-microtrichia, pfx-posterior flexing patch, psfd-posterior subcostal field, ptst-pterostigma, rs-"radial sector", scr-subcostal ridge 2, 3 Pulvinaria vitis (Linnaeus): scanning electron microphotographs of the wing, showing its microsculpture 4, 5 Male of Pulvinaria vitis (Linnaeus) on white background, with invisible WIPs, and 2 on a black background, showing WIPs.
Figures 6-13 from: Simon E (2013) Preliminary study of wing interference patterns (WIPs) in some species of soft scale (Hemiptera, Sternorrhyncha, Coccoidea, Coccidae). ZooKeys 319: 269-281. https://doi.org/10.3897/zookeys.319.4219
Figures 6-13 - Males with "horizontally striped patterns" of WIPs, subfamilies Eulacaninae and Coccinae: 6–7 WIP of Sphaerolecanium prunastri (Boyer de Fonscolombe) 8–9 WIP of Eulecanium tiliae (Linnaeus) 10, 11 WIP of Pulvinaria vitis 12–13 WIP of Parthenolecanium corni (Bouché).
Data for: Properties of wing scales on butterflies with different distribution patterns
<p><span>Butterflies play a crucial role in understanding the spread of life due to their complex thermal adaptations. </span><span>The cooling capacity provided by wing scales</span><span> is a dominant factor associated with the ambient temperature of their habitats. </span><span>However, it remains unclear how the wing scale structure of butterflies varies to regulate cooling capacity and participate in shaping distribution patterns.</span></p> <p><span>Based on data acquired from quantitative measurements, rank sum and ANOVA tests were used to test whether the structure and cooling capacity of wing scales responded to butterfly distribution. Virtual simulations and Spearman tests were used to confirm the correlation between the structure and cooling capacity of wing scales. The response was first resolved using three representative species with gradient differences in distribution, and then macroscopically validated using 99 species</span><span> within</span><span> their phylogenetic framework, with a presampling control to exclude potential effects of taxonomic position, body size, and migratory behaviour.</span> <span>Both optical and thermal properties were used to measure the cooling capacity. Thermal data generated from specimens in different states were used to exclude the effects of other thermoregulatory pathways.</span></p> <p><span>The results show that the cooling capacity of butterfly wings decreases and becomes more homogeneous as the temperature of their habitat decreases. The decrease in cooling capacity is due to the decrease in maximum emissivity, while the homogenisation is due to both the decrease in maximum emissivity and the increase in minimum emissivity. Variation in cooling capacity is due to changes in the structure of wing scale, which homogenises as the habitat becomes colder. As butterflies generally spread from the tropics to temperate zones, it is inferred that the generation of a low overall cooling capacity through structural homogenisation of wing scales has supported the dispersal of butterflies.</span></p> <p><span>For the first time, we provide cascading evidence for the links between butterfly distribution, thermal adaptation, and functional morphology. We also highlight the role of structural homogenisation on the poikilothermic body surface in the adaptive process for dispersal. Further investigation using genetic information would be beneficial to resolve the mechanism behind thermal adaptation at a deeper level.</span></p>
Data for: Properties of wing scales on butterflies with different distribution patterns
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Data in support of Patterns of parental care and movement in divided broods of Golden-winged Warblers
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The roles of wing color pattern and geography in the evolution of Neotropical Preponini butterflies
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Relating wing morphology and immune function to patterns of partial and differential bat migration using stable isotopes
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Patterns of genetic divergence and demographic history shed light on island-mainland population dynamics and melanic plumage evolution in the white-winged fairywren
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Data from: Evolutionary novelty in a butterfly wing pattern through enhancer shuffling
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Common genome-wide patterns of transcript accumulation underlying the wing polyphenism and polymorphism in the pea aphid
GEO Series GSE8008. Buchnera aphidicola; Escherichia coli; Acyrthosiphon pisum. 24 samples. Type: Expression profiling by array.
Butterfly wing pattern mimicry radiated via parallel evolution of ancient, pleiotropic enhancers [HiC-seq]
GEO Series GSE123703. Heliconius erato lativitta. 4 samples. Type: Other.
De novo transcriptome analysis profiles gene expression underlying seasonal polyphenism in butterfly wing patterns
GEO Series GSE54819. Junonia coenia. 20 samples. Type: Expression profiling by high throughput sequencing.
De novo transcriptome analysis profiles gene expression in Vanessa cardui wing patterns
GEO Series GSE78119. Vanessa cardui. 14 samples. Type: Expression profiling by high throughput sequencing.
Fig. 7 in Phylogeny of Eulithis Hübner and Related Genera (Lepidoptera: Geometridae), with an Implication of Wing Pattern Evolution
Fig. 7. Wing venation of Eustroma (= Antepirrhoe) semiatratum. Scale bar = 1 mm.
Butterfly wing pattern mimicry radiated via parallel evolution of ancient, pleiotropic enhancers [ChIP-Seq]
GEO Series GSE123701. Heliconius erato lativitta. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Butterfly wing pattern mimicry radiated via parallel evolution of ancient, pleiotropic enhancers [ATAC-Seq]
GEO Series GSE123700. Heliconius melpomene aglaope; Heliconius melpomene rosina. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
FIGURES 2–18. Wing patterns. 2–3 in A taxonomic review of the genus Amicta Heylaerts, 1881 in North Africa, Near and Middle East (Lepidoptera, Psychidae, Oiketicinae, Acanthopsychini)
FIGURES 2–18. Wing patterns. 2–3: Amicta murina (2: add country, add locality; 3: Holotype, Egypt (MfN)); 4: A. bouhedmaensis (Holotype Tunisia, Degache, (MWM); 5–7: A. maliarda (5: Algerie, südl. Biskra (MWM) (prep. 2294/2020, Rajaei); 6: Tunesien, Kasserine, Ri Chambi NP, (CTS) (prep. 123-2021 Sobczyk).; 7: Libya, Sinauen, (MWM) (prep. 2292/2020, Rajaei) 8–9: A. lutensis sp. nov. (8: Holotype Iran, Lut desert, 20 km N Bam, Shahrokh-Abad, N29°17'22.2" E59°05'27.8" (SMNS); 9: Paratype, same data as holotype; 10: A. chambiana sp. nov. (Holotype Tunisia, ca. 10 km W Kasserine, near Chambi NP); 11: A. mauretanica (Holotype, Algeria, Bou Saada (NHM); 12: A. arabica (Oman, N of Sur, near Fins, coast line, 15.xi.2017, N 22°53.630', E 059°13.371); 13: A. quadrangularis (Turkmenistan, Krasnowodsk, Transcaspia, Krasnowodsk mys Sarta (MWM) (prep. 4126 Arnscheid); 14–15: A. nigrescens (14: Syntype [labeled as Origin by Staudinger], Caucasus, Ordubat; 15: Afghanistan, Kabul (MWM); 16: A. sericata (Iran, Ghatrouyeh, Neyriz, 1580 m, Fars Provinz, 54°42'E, 29°08'N); 17-A: A. davarica (Holotype Iran, Hormozgan prov., Beshagerd Mts. Davari vil., 26°27' N 57°38'E, 06.-11.04.2000); 17-B: A. acutella (Krüger, 1939: pl. 14). a, upperside; b, underside. Scale-bar 1 cm.
FIGURES 20-37. Wing pattern. 20 in An integrative taxonomic revision of the genus Triphosa Stephens, 1829 (Geometridae: Larentiinae) in the Middle East and Central Asia, with description of two new species
FIGURES 20-37. Wing pattern. 20: Philereme transversata (Germany, Augsburg, 12.vii.1970; SMNS); 21: Pareulype berberata (Germany, Mannheim, 13.vii.1933; SMNS); 22: Triphosa dubitata (Georgia, Borjomi, 22.vii.2006, g. prep. 0016/ 2018 D. Wanke); 23-24: Triphosa silviae sp. n. (23: holotype, Iran, Fars, v.1937, g. prep. 0059/2018 D. Wanke; 24: paratype, Iran, Fars, Tange Surkh, g. prep. 755/2009 H. Rajaei); 25-26: Triphosa lecerfi sp. n. (25: holotype, Alai, Dugoba, 27.vii.1993, g. prep. 0042/2018 D. Wanke; 26: paratype, Alai, Dugoba, 27.vii.1993, g. prep. 0041/2018 D. Wanke); 27: holotype of Triphosa agnata syn. n. of Triphosa sabaudiata (Turkey, Cesarée, g. prep. 223); 28-30: Triphosa sabaudiata (28: Germany, Herrlingen, Tiefental; 29: Germany, Gempen, i.1959, g. prep. 0052/2018 D. Wanke; 30: Gempen, 25.vii.1955, g. prep 0005/ 2018 D. Wanke); 31-32: female 'syntypes' of Triphosa taochata (31: lectotype here designated, Azerbaijan, Hankynda; 32: paralectotype, Georgia, Achalziche); 33-34: Triphosa taochata (both Iran, Elburs, Damavand, 11.vii.1972; 33: g. prep 0012/ 2018 D. Wanke; 34: g. prep 0011/2018 D. Wanke); 35: Rheumaptera hastata (Germany, Federseemoor, 30.v.1967); 36: Hydria cervinalis (Germany, Heidelberg, 29.iii.1974, g. prep. 0051/2018 D. Wanke); 37: lectotype of Hydria ravulata (Issyk-kul, g. prep. 0048/2018 D. Wanke). a = upperside; b = underside.
Figures 67–90. Male fore wing pattern. Figures 67, 68 in Taxonomic revision of the genus Delorhachis Karsch 1896 (Lepidoptera: Limacodidae)
Figures 67–90. Male fore wing pattern. Figures 67, 68: Delorhachis viridiplaga; Figure 69: D. charopa stat. rev.; Figure 70: D. ochsei sp. nov.; Figures 71, 72: D. chlorodaedala; Figure 73: D. kitale; Figure 74: D. tommasoi sp. nov.; Figure 75: D. pallidifascia sp. nov.; Figure 76: D. mariae; Figure 77: D. parvinota sp. nov.; Figures 78, 79: D. meyi sp. nov.; Figure 80: D. wetzelae sp. nov.; Figure 81: D. wetzelae shambaa ssp. nov.; Figure 82: D. kilosa; Figure 83: D. zambica sp. nov.; Figure 84: D. syntomoctena comb. nov.; Figure 85: D. manuelae sp. nov.; Figure 86: D. bakossii sp. nov.; Figure 87: D. smithi sp. nov.; Figure 88: D. nimbaensis sp. nov.; Figure 89: D. baaka sp. nov.; Figure 90: D. nigrivenosa.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
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The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
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